Canonical Allele Identifier: CA366234198

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510874T>G (hg19) ; chr6:g.157189740T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189740T>G , CM000668.2:g.157189740T>G	GRCh38
NC_000006.11:g.157510874T>G , CM000668.1:g.157510874T>G	GRCh37
NC_000006.10:g.157552566T>G	NCBI36
NG_032093.1:g.416811T>G
NG_032093.2:g.416811T>G
NG_066624.1:g.418715T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3859T>G	ENSP00000055163.8:p.Ser1287Ala
ENST00000414678.8:c.3928T>G	ENSP00000412835.3:p.Ser1310Ala
ENST00000637015.2:c.4147T>G	ENSP00000489729.2:p.Ser1383Ala
ENST00000346085.10:c.3898T>G	ENSP00000344546.5:p.Ser1300Ala
ENST00000350026.10:c.3610T>G	ENSP00000055163.7:p.Ser1204Ala
ENST00000414678.7:c.2176T>G	ENSP00000412835.2:p.Ser726Ala
ENST00000635849.1:c.1339T>G	ENSP00000490948.1:p.Ser447Ala
ENST00000635957.1:c.973T>G	ENSP00000490385.1:p.Ser325Ala
ENST00000636930.2:c.4018T>G MANE Select	ENSP00000490491.2:p.Ser1340Ala
ENST00000636940.1:n.2015T>G
ENST00000637015.1:c.1386T>G
ENST00000637568.1:c.1300T>G
ENST00000637741.1:n.684T>G
ENST00000637810.1:c.1360T>G	ENSP00000489636.1:p.Ser454Ala
ENST00000637904.1:c.1519T>G	ENSP00000490550.1:p.Ser507Ala
ENST00000647938.1:c.3649T>G	ENSP00000498155.1:p.Ser1217Ala
ENST00000346085.9:c.3649T>G	ENSP00000344546.4:p.Ser1217Ala
ENST00000350026.9:c.3610T>G	ENSP00000055163.7:p.Ser1204Ala
ENST00000414678.6:c.2176T>G	ENSP00000412835.2:p.Ser726Ala
NM_017519.2:c.3610T>G	NP_059989.2:p.Ser1204Ala
NM_020732.3:c.3649T>G	NP_065783.3:p.Ser1217Ala
XM_005267069.3:c.3769T>G	XP_005267126.2:p.Ser1257Ala
XM_011535984.1:c.2848T>G	XP_011534286.1:p.Ser950Ala
XM_011535985.1:c.2668T>G	XP_011534287.1:p.Ser890Ala
XM_011535986.1:c.2428T>G	XP_011534288.1:p.Ser810Ala
XM_011535987.1:c.2047T>G	XP_011534289.1:p.Ser683Ala
XM_011535988.1:c.910T>G	XP_011534290.1:p.Ser304Ala
NM_001346813.1:c.3769T>G	NP_001333742.1:p.Ser1257Ala
NM_001363725.1:c.1519T>G	NP_001350654.1:p.Ser507Ala
XM_011535984.2:c.3979T>G	XP_011534286.2:p.Ser1327Ala
XM_011535988.3:c.910T>G	XP_011534290.1:p.Ser304Ala
XM_017011103.2:c.3880T>G	XP_016866592.1:p.Ser1294Ala
XM_017011104.1:c.3850T>G	XP_016866593.1:p.Ser1284Ala
XM_017011105.2:c.3820T>G	XP_016866594.1:p.Ser1274Ala
XM_017011106.2:c.3691T>G	XP_016866595.1:p.Ser1231Ala
XM_017011107.2:c.3670T>G	XP_016866596.1:p.Ser1224Ala
XR_002956289.1:n.4062T>G
NM_001363725.2:c.1519T>G	NP_001350654.1:p.Ser507Ala
NM_001371656.1:c.3898T>G	NP_001358585.1:p.Ser1300Ala
NM_001374820.1:c.3898T>G	NP_001361749.1:p.Ser1300Ala
NM_001374828.1:c.4018T>G MANE Select	NP_001361757.1:p.Ser1340Ala
NM_017519.3:c.3859T>G	NP_059989.3:p.Ser1287Ala